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“Pulsating proptosis and heavy eye syndrome precipitated by neurofibromatosis type 1: A case report”

RATIONALE: Neurofibromatosis type 1 (NF1) is a hereditary disease characterized by café-au-lait spots, peripheral neurofibromas, Lisch nodules, optic nerve glioma, and sphenoid wing dysplasia. Pulsating proptosis is associated with a sphenoid bony defect. Heavy eye syndrome is characterized by acqui...

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Detalles Bibliográficos
Autores principales: Lai, Yi-Fen, Lee, Lung-Chi, Chen, Yi-Hao, Chien, Ke-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542118/
https://www.ncbi.nlm.nih.gov/pubmed/34678901
http://dx.doi.org/10.1097/MD.0000000000027575

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